Allele Registry

Canonical Allele Identifier: PA2828094892

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042587

RCV001383217

ClinVar Variation:

49327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.His1554Tyr	CA021147 NM_001363528.2:c.4660C>T